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1 OMIM reference -
2 associated genes
4 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
4 associated genes
No signs/symptoms info
Persistent Müllerian duct syndrome
Squamous cell carcinoma of head and neck

AMH ING1
AMHR2 ING3
PTEN
TNFRSF10B


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
AMHR2
(0.63)
PTEN



Citations in the biomedical literature:


Persistent Müllerian duct syndrome
AMH AMHR2
Squamous cell carcinoma of head and neck
ING1 ING3 PTEN TNFRSF10B



Persistent Müllerian duct syndrome
Squamous cell carcinoma of head and neck

Synonym(s):
- PMDS
- Persistent Müllerian derivatives

Synonym(s):
- HNSCC
- Head and neck squamous cell carcinoma

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare infertility
- Rare urogenital disease
Classification (Orphanet):
- Rare oncologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
1 MeSH reference: C536665
External references:
1 OMIM reference -
1 MeSH reference: C535575

Persistent Müllerian duct syndrome

Very frequent
- Autosomal recessive inheritance
- Undescended / ectopic testes / cryptorchidia / unfixed testes

Frequent
- Inguinal / inguinoscrotal / crural hernia
- Male pseudohermaphrodism / lack of virilisation



Squamous cell carcinoma of head and neck

(no data available)